Orphanet: SPG21
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SPG21 - SPG21 abhydrolase domain containing, maspardin

  • Synonym(s) : ABHD21, ACP33, BM-019, GL010, MAST
  • Previous symbols and names : SPG21, maspardin, spastic paraplegia 21 (autosomal recessive, Mast syndrome)
  • Type : gene with protein product
  • Chromosomal location : 15q22.31
  • OMIM: 608181
  • HGNC: 20373
  • UniProtKB: Q9NZD8
  • Genatlas: SPG21
  • Ensembl: ENSG00000090487
  • IUPHAR-DB: -
  • Reactome: Q9NZD8
  • LOVD: SPG21

Diseases list

  : Assessed

Gene included in a panel of genes performed as part of a diagnostic test


Additional information

Health care resources for this gene

Specialised Social Services

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